| Property | Value |
|---|
| Working Groups |  RG Wollnik |
| Subproject | None |
| Open Access |  Yes |
| Publication Type | Journal Article |
| Peer Reviewed | Yes |
| PMID |  37352860 |
| DOI |  10.1016/j.ajhg.2023.06.001 |
| Publication Year | 2023 |
| Title | Null and missense mutations of ERI1 cause a recessive phenotypic dichotomy in humans |
| Journal | American Journal of Human Genetics |
| ISSN | 0002-9297 |
| eISSN | 1537-6605 |
| URL | https://doi.org/10.1016/j.ajhg.2023.06.001 |
| Pages | 1068-1085 |
| Issue | 7 |
| Volume | 110 |
| Journal Abbreviation | Am J Hum Genet |
| Authors | Guo L, Salian S, Xue J, Rath N, Rousseau J, Kim H, Ehresmann S, Moosa S, Nakagawa N, Kuroda H, Clayton-Smith J, Wang J, Wang Z, Banka S, Jackson A, Zhang Y, Wei Z, Hüning I, Brunet T, Ohashi H, Thomas MF, Bupp C, Miyake N, Matsumoto N, Mendoza-Londono R, Costain G, Hahn G, Di Donato N, Yigit G, Yamada T, Nishimura G, Ansel KM, Wollnik B, Hrabě de Angelis M, Mégarbané A, Rosenfeld JA, Heissmeyer V, Ikegawa S, Campeau PM |
| First Author | Guo L |
| Last Author | Campeau PM |
External Resources
gro-2/129327http://resolver.sub.uni-goettingen.de/purl?gro-2/129327
GRO.publications identifier
